BioTalent
We’re seeking a Senior Design Quality Engineer to support product design, development, and manufacturing of electronic and electromechanical medical devices. This role ensures compliance with QMS, ISO, and FDA regulations while driving quality across development and commercial operations.
To be considered for an interview, please make sure your application is full in line with the job specs as found below. Overview The successful candidate will lead quality efforts on cross-functional project teams for new and existing products, support design control, risk management, and product verification/validation, develop and validate test methods, inspection procedures, and quality standards, analyze non-conformances, lead investigations, and support CAPA/NCR boards, prepare documentation and support audits (FDA, FDB, notified body), provide training, guidance, and mentorship to team members, and collaborate with contract manufacturers on electromechanical devices and PCBAs. Key Responsibilities Lead quality efforts on cross-functional project teams for new and existing products Support design control, risk management, and product verification/validation Develop and validate test methods, inspection procedures, and quality standards Analyze non-conformances, lead investigations, and support CAPA/NCR boards Prepare documentation and support audits (FDA, FDB, notified body) Provide training, guidance, and mentorship to team members Collaborate with contract manufacturers on electromechanical devices and PCBAs Qualifications Bachelor’s degree in Engineering, Life Science, or related field (advanced degree preferred) 5+ years of quality assurance experience in medical devices or regulated industry Hands-on experience with PFMEA, NCRs, CAPAs, change control, and failure investigations Familiarity with electronics/PCBA manufacturing and contract manufacturing Background in auditing, sterilization, design reviews, and/or project management Working Conditions Mix of office, lab, and cleanroom environments Limited travel (0–10%) Ability to lift up to 25 lbs and support inspections, audits, and hands-on testing Compensation:
$150,000 – $170,000 Location:
SF Bay Area
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To be considered for an interview, please make sure your application is full in line with the job specs as found below. Overview The successful candidate will lead quality efforts on cross-functional project teams for new and existing products, support design control, risk management, and product verification/validation, develop and validate test methods, inspection procedures, and quality standards, analyze non-conformances, lead investigations, and support CAPA/NCR boards, prepare documentation and support audits (FDA, FDB, notified body), provide training, guidance, and mentorship to team members, and collaborate with contract manufacturers on electromechanical devices and PCBAs. Key Responsibilities Lead quality efforts on cross-functional project teams for new and existing products Support design control, risk management, and product verification/validation Develop and validate test methods, inspection procedures, and quality standards Analyze non-conformances, lead investigations, and support CAPA/NCR boards Prepare documentation and support audits (FDA, FDB, notified body) Provide training, guidance, and mentorship to team members Collaborate with contract manufacturers on electromechanical devices and PCBAs Qualifications Bachelor’s degree in Engineering, Life Science, or related field (advanced degree preferred) 5+ years of quality assurance experience in medical devices or regulated industry Hands-on experience with PFMEA, NCRs, CAPAs, change control, and failure investigations Familiarity with electronics/PCBA manufacturing and contract manufacturing Background in auditing, sterilization, design reviews, and/or project management Working Conditions Mix of office, lab, and cleanroom environments Limited travel (0–10%) Ability to lift up to 25 lbs and support inspections, audits, and hands-on testing Compensation:
$150,000 – $170,000 Location:
SF Bay Area
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